Canonical Allele Identifier: CA602136478

Gene: APOA1

Linked Data

• dbSNP Id: rs1565338304
• gnomAD v2: 11-116706478-GA-G
• gnomAD v4: 11-116835762-GA-G
• MyVariant Identifiers: chr11:g.116706479del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116835765del , CM000673.2:g.116835765del	GRCh38
NC_000011.9:g.116706481del , CM000673.1:g.116706481del	GRCh37
NC_000011.8:g.116211691del	NCBI36
NG_012021.1:g.6860del , LRG_767:g.6860del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236850.5:c.*45del MANE Select	ENSP00000236850.3:n.*45del
ENST00000236850.4:c.*45del	ENSP00000236850.3:n.*45del
ENST00000359492.6:c.*45del	ENSP00000352471.2:n.*45del
ENST00000375320.5:c.*45del	ENSP00000364469.1:n.*45del
ENST00000375323.5:c.*45del	ENSP00000364472.1:n.*45del
ENST00000375329.6:c.*45del	ENSP00000364478.2:n.*45del
NM_000039.1:c.*45del , LRG_767t1:c.*45del	NP_000030.1:n.*45del
XM_005271539.2:c.*45del	XP_005271596.1:n.*45del
XM_005271540.1:c.*45del	XP_005271597.1:n.*45del
NM_000039.2:c.*45del	NP_000030.1:n.*45del
NM_001318017.1:c.*45del	NP_001304946.1:n.*45del
NM_001318018.1:c.*45del	NP_001304947.1:n.*45del
NM_001318021.1:c.*45del	NP_001304950.1:n.*45del
NM_001318017.2:c.*45del	NP_001304946.1:n.*45del
NM_001318018.2:c.*45del	NP_001304947.1:n.*45del
NM_000039.3:c.*45del MANE Select	NP_000030.1:n.*45del